Plasma-assisted CuO/CeO2/TiO2-γ-Al2O3 catalysts for NO+CH4 reaction and NO temperature programmed desorption studies
•Plasma-assisted CuO-based catalysts system with NO+CH4 reaction is studied.•CuO/CeO2/TiO2/γ-Al2O3 catalysts has the best NO removal activity among four catalysts.•NO conversion decreases in the order of CuO/CeO2/TiO2/γ-Al2O3 >CuO/TiO2/γ-Al2O3.•CuO/γ-Al2O3>CuO/TiO2.•H2-TPR and NO-TPD explain t...
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Published in | Applied surface science Vol. 280; pp. 273 - 281 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
01.09.2013
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •Plasma-assisted CuO-based catalysts system with NO+CH4 reaction is studied.•CuO/CeO2/TiO2/γ-Al2O3 catalysts has the best NO removal activity among four catalysts.•NO conversion decreases in the order of CuO/CeO2/TiO2/γ-Al2O3 >CuO/TiO2/γ-Al2O3.•CuO/γ-Al2O3>CuO/TiO2.•H2-TPR and NO-TPD explain the reason for CuO/CeO2/TiO2/γ-Al2O3 better NO removal.
The removal of NO and CH4 has been studied with a hybrid system integrating plasma activation and four Cu-based catalysts. The best catalytic performance was observed for catalysts obtained from CuO/CeO2/TiO2/γ-Al2O3.The efficiency of NO removal decreased with the order: 12%CuO/10%CeO2/15%TiO2/γ-Al2O3>12%CuO/15%TiO2/γ-Al2O3>12%CuO/γ-Al2O3>12% CuO/TiO2. Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD) Temperature-programmed reduction (H2-TPR) and NO temperature-programmed desorption (NO-TPD) experiments were carried out to gain insight into the synergetic effects with the catalysts. The results revealed that copper species existed as bulk CuO crystalline for all the catalysts, H2-TPR suggested that the Cu2+ incorporated TiO2 or CeO2 lattice and crystalline CuO might be the most active component for NO removal, and NO-TPD studies indicated that 12%CuO/10%CeO2/15%TiO2/γ-Al2O3 catalyst had lower NO desorption temperature and larger peak area, which seemed to be responsible for the better catalytic activity over NO+CH4 reactions than other catalysts. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2013.04.149 |